• Ads by Google:
     




    Get email alerts Celiac.com E-Newsletter

    Ads by Google:



       Get email alertsCeliac.com E-Newsletter

  • Announcements

    • admin

      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to FREE Celiac.com email alerts   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes Where can I buy gluten-free stuff? Support this site by shopping at The Celiac.com Store.

Seattle Area Anyone?
0

16 posts in this topic

Recommended Posts

pborschowa    0

Just wondering if there is anyone from the seattle area on here???

Share this post


Link to post
Share on other sites
Ads by Google:
Ads by Google:


tarnalberry    314
Just wondering if there is anyone from the seattle area on here???

I am now! (moved up here three months ago)

Share this post


Link to post
Share on other sites
Just wondering if there is anyone from the seattle area on here???

I live in Seattle. I've also been looking for others in Seattle that frequent this forum. How long have you been gluten free? I'm on yahoo messenger as massage45678 if you want to chat.

Share this post


Link to post
Share on other sites
Ads by Google:


BB22    0

Hi,

I too am in Seattle, north end.

Do y'all go to any of the local support groups? Or is this the place?

bb22

Share this post


Link to post
Share on other sites
lonewolf    0

I'm in Federal Way. One of my children is gluten-free too. Just went to Kaili's kitchen in Edmonds today. It was a little, let's say, informal, but sure was nice to have fish and chips for the first time in 10 years.

Liz

Share this post


Link to post
Share on other sites


Ads by Google:


burdee    80

Hi All of You in the Seattle Area:

I LEAD A CELIAC SUPPORT GROUP WHICH MEETS IN BOTHELL (NORTH SEATTLE AREA) on every 2nd Tuesday of the Month. We meet next on Valentine's Day (February 14) 7-8:30pm. We will have free NAMASTE gluten-free goody samples and discuss 'Travelling with celiac disease'. If you're interested, email me, penguinea@hotmail.com and I'll send you directions to our meeting location. Our group is called 'SNOCOCELIACS' because we used to meet at "Kaili's Kitchen" in Snohomish County. When I assumed leadership last August, I chose a nonrestaurant location to eliminate restaurant noise distractions during our discussions.

If 2nd Tuesdays don't work for you or if you would prefer an Eastside (Bellevue/Redmond) location, another group which calls themselves "Seattle Celiacs" (yeah, that's confusing) meets on 3rd Tuesdays at the Group Health Eastside Hospital from 7-9pm. Contact earl.ley@comcast.net. He leads that group.

BURDEE

Share this post


Link to post
Share on other sites
RussCourt    0

I'm live in Bellevue...just moved here with my DF three weeks ago. I'm not officially gluten-free yet (tried an elimination diet, found some positive results, but waiting until I have Enterolab or similar to go off officially), but I would love to hang out and talk with other Seattle-area gluten-free folk. I have had eczema since I was an infant, IBS since 17 or so, and after I moved to Russia for six months, an explosion of systems, mostly related to pain/cramping/heaviness in legs and arms, breathlessness, bloatedness, and anxiety. Getting an EKG in Moscow....quite the adventure! I also have a family history of GI problems, anemia and infertility. I like the idea of drug-free treatments, so if the tests turn up even suggestive of gluten intolerance...I'm done with it.

I'd love to stop by these groups. Thanks for letting us know about them! :)

Share this post


Link to post
Share on other sites
mitch    0
I live in Seattle. I've also been looking for others in Seattle that frequent this forum. How long have you been gluten free? I'm on yahoo messenger as massage45678 if you want to chat.

I live in sammamish I was just diagnosed three weeks ago with celiac's. It really sucks so basiclly i have only been gluten free for three weeks.

Share this post


Link to post
Share on other sites


Ads by Google:


mamaw    133

I was in Seattle last year for vacation. Loved it there.......I will vouch for Mona's mixes from Woodinville. Her pancake mix is the very best I have ever eaten.....I tried to contact Kailli's place but she just about hung up in m y ear so I can't say I was impressed with her. Maybe she was having a bad day ..........She was the first celiac that wasn't friendly and helpful ......

By the way Lisa from Mona's mixes contacted me immediately after I left her a message and she is very polite and friendly...

mamaw

Share this post


Link to post
Share on other sites

Hello Everyone!

I live in Kirkland, which is in the Greater Seattle area. I suspected I had celiac disease now for the last year or more, but I just received my results from the biopsy via the mail today, Yippee.

/wave

My first post here...

:unsure:

Share this post


Link to post
Share on other sites
BRUMI1968    7

I lived on Cap Hill for several years...now I live in Bellingham (1.5 hours north). I don't miss Seattle traffic, noise, or smell...but other than that. I miss Lake Union, and rowing, and restaurants that are open late, and "Whole Paycheck..." I mean, Whole Foods.

B-ham is great, though. Got the fresh air, enough dogs to satisfy anyone (even me), trails, mountains, skiing, Vancouver BC...yeah, I like Bellingham.

All you Seattle-area-ites should make a trip up here and we can all go on a Celiac hike in the Chuckanuts.

Welcome, anyway, though I see it was months ago you started this post.

Yeah, Seattle! (I read that Seattle was voted #2 good eatin by PETA - lost to San Francisco but beat out New York for place 2...never mind PETA makes me cranky, that's another story.)

Share this post


Link to post
Share on other sites

Can anyone confirm that Kaili's kitchen or Kaili's Bakery has moved to;

10003 Greenwood Ave N

Seattle, WA 98133

I haven't been there yet and would like to try it out!

-Thanks

Share this post


Link to post
Share on other sites


Ads by Google:


AndreaB    1
I lived on Cap Hill for several years...now I live in Bellingham (1.5 hours north). I don't miss Seattle traffic, noise, or smell...but other than that. I miss Lake Union, and rowing, and restaurants that are open late, and "Whole Paycheck..." I mean, Whole Foods.

B-ham is great, though. Got the fresh air, enough dogs to satisfy anyone (even me), trails, mountains, skiing, Vancouver BC...yeah, I like Bellingham.

All you Seattle-area-ites should make a trip up here and we can all go on a Celiac hike in the Chuckanuts.

Welcome, anyway, though I see it was months ago you started this post.

Yeah, Seattle! (I read that Seattle was voted #2 good eatin by PETA - lost to San Francisco but beat out New York for place 2...never mind PETA makes me cranky, that's another story.)

Bully4You,

I like Bellingham as well. I went to WWU for 2 + years up there. Very pretty area. Now I live about 30 minutes from Vancouver WA. Another pretty area but not as picturesque as Bellingham. I would love to try and get to NE Washington but jobs aren't very plentiful there and my hubby is the only income earner as I stay home with the kiddies.

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

0

  • Forum Statistics

    • Total Topics
      107,886
    • Total Posts
      938,474
  • Member Statistics

    • Total Members
      65,789
    • Most Online
      3,093

    Newest Member
    Grayskull
    Joined
  • Popular Now

  • Topics

  • Posts

    • I need an anti inflammatory gluten free brand. Or something like Tylenol. I am in pain and do not want to take heavy prescriptions. Anyone know what is gluten-free and if and how bad they are for digestion. Advil, Aleve, motrin or Tylenol. I know the NSAID's are the advil and aleve what do people prefer most. I know there are some of you out there with joint and bone pain.
    • Ennis I looked up the nutritional deficiency list you posted. The only ones I was tested for was b1 (three numbers away from being out of range low), b2, b3 there was none detected in my system and I asked my doctor about this and he said its not accurate and never told me what to do about it. Vit E was fine along with magnesium but vit A was very low like one number away from deficiency. These were all checked in March so I am hoping some numbers went up, like my iron panel was severely low when first tested but has gone up to normal numbers except the ferritin. Which my doctor told me don't worry about. The other nutrients I have yet to get tested and hate that doctors only like to test for vit d ( that was insufficient last time and has gone up, from 20 to 43  and b12 which was 200 and has gone up to 400 (Ive been getting monthly injections). Which I don't think has done much of anything.
    • Why not just ask her?  She is a very nice doctor .  You should be able to find her    i mean Jess- the patient Celiac
    • Yes Plumbago, my Neutrophils are low in particular. I'm not on any medications or have a rash. No one in my family has auto immune problems except my great grandmother who had Rheumatoid arthritis so bad she had to move out west for the better weather. What does the urinalysis show? I had my ANA tested, twice (lol).  I just feel completely sick and fatigue. I cant even explain it to doctors just a general feeling of malaise. Its up and down throughout the day. My blood pressure is extremely low in the middle of the night. I almost pass out going to the bathroom every night it is like clock work. The breathing problem makes me think allergies because I have a deviated septum and have constant nasal congestion and mucus in my throat. I wish I knew exactly what was making me feel so sick. And I am at a loss for the low WBC. It didn't just show up low once but three times this past year and a half. Does anyone know about anything with High methane in the breath?
    • Forum Members, This is a follow up question to a link posted in this thread I have read the Patient Celiac site before but she noted the possible use of Losartan (Potassium) contributing to Villi Blunting? This concerns me because I am now taking Losartan for blood pressure. Can any one describe their experience with Losartan and/or provide the link that states Losartan's could be a contributing factor in Villi Blunting. The Patient Celiac did not site her source and I couldn't find it.  Any help as to the source would be helpful because I would like to read it for myself. Also what other blood pressure medicine's do others on this forum take instead of Losartan. My BP seems to be under control now that I have been taking Folic Acid but don't won't to stop cold turkey until I have another BP medicine I can take in it's place that won't contribute to possible Villi Blunting. I recently had to "catch up" on Vitamin D for my prediabetes so I know absorption is still a problem and thought it  was curious because years ago after my celiac diagnosis I had caught up on Vitamin D once before so I was surprised to find I was again low in it again. The Losartan and Villi blunting (if indeed they are linked) could explain why I am still low (again) in Vitamin D. I knew NSAIDS could cause and why I don't take them generally unless I am in unbearable pain but wasn't aware common BP medicines other than Benicar (olmesartan) could cause similar villi blunting. Here is the link on the NSAIDs study. http://www.thedailybeast.com/research-shows-link-between-nsaid-use-and-gut-disease but the cureceliac.org site does not mention Losartan as other causes of Villi Blunting. http://www.cureceliacdisease.org/faq/what-else-can-cause-damage-to-the-small-intestine-other-than-celiac-disease/ So does any body know if Losartan has also been linked to Villi blunting. If it has I need to get off of it for good and find another BP medicine without this severe side effect. Thanks in Advance.  posterboy,  
  • Upcoming Events